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| Introduction |
Unit 1
Welcome/Historical Perspective/Choosing a Research Question
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John I. Gallin, M.D.
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| Module I - Statistical Methods |
Unit 2
Participant Selection
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Running Time: 2:50:37
Tamara Harris, M.D., M.S.
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Using Secondary Data and Meta Analysis
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Running Time:
Tamara Harris, M.D., M.S.
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Unit 4
Design of Epidemiologic Studies
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Running Time: 2:49:52
Laura Lee Johnson, Ph.D.
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Unit 6
Economic Analysis in Clinical Research
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Running Time: 2:50:51
Martin Brown, Ph.D.
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Unit 7
Study Development
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Running Time: 1:21:22
Laura Lee Johnson, Ph.D.
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Unit 8
Issues in Randomization
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Running Time: 1:22:52
Laura Lee Johnson, Ph.D.
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Unit 9
Overview of Hypothesis Testing
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Running Time: 1:25:44
Laura Lee Johnson, Ph.D.
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Unit 10
Sample Size and Power
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Running Time: 1:30:02
Laura Lee Johnson, Ph.D.
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Unit 11
Conceptual Approach to Survival Analysis
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Running Time: 1:25:27 minutes
Laura Lee Johnson, Ph.D.
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Unit 12
Designing and Testing Questionnaires
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Running Time: 57:48 minutes
Jack Guralnik, M.D., Ph.D.
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Unit 13
Ethical Principles in Clinical Research
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Running Time: 1:02:26
Christine Grady, R.N., Ph.D.
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Opportunities for Innovation in Clinical Research: From Molecule to Medicare - Parts I & II
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Running Time: 33:57
Mitchell Max , M.D. & Joanne Lynn
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| Module II - Ethical Issues and Regulation of Human Subjects Research |
Unit 1
Researching an Ethics Question
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Ezekiel Emanuel, M.D., Ph.D.
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Concepts in the Management of Projects
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Running Time:
Charles Grudzinskas, Ph.D.
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Unit 3
Legal Issues in Clinical Reseach
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Running Time: 1:04:20
Valerie Bonham, J.D.
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Concepts in the Management of Projects
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Running Time:
Charles Grudzinskas, Ph.D.
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Unit 5
Evaluation of a Protocol Budget
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Running Time: 1:00:57
Margaret Matula, B.S.N., M.G.A.
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Unit 6
Special Lecture: Human Genome Project and Clinical Research
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Running Time: 1:04:42
Christopher Austin, M.D.
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| Module III - Monitoring Patient-Oriented Research and Regulatory Issues |
Unit 1
FDA Product Regulation
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Running Time: 1:08:33
Robert Yetter, Ph.D.
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Unit 2
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Unit 4
Data and Safety Monitoring in Clinical Trials
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Running Time: 1:00:55
Dennis O. Dixon, Ph.D.
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Unit 5
Data Management in Clinical Trials
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Running Time: 55:33
Diane St. Germain, R.N., M.S.N., C.R.N.P.
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Unit 6
Quality Control in Clinical Trials
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Running Time: 46:07
Jack Guralnik, M.D., Ph.D.
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Unit 7
Quality of Life
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Running Time: 1:11:27
John Ware, Ph.D.
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| Module IV - Preparing and Funding a Clinical Research Study |
Unit 1
Scientific Conduct
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Running Time: 44:12
Joan Schwartz, Ph.D.
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The Clinical Researcher and the Media
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Running Time: 36:36
John Burklow, M.S.
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Unit 2
ProtoType and Protocol Mechanics
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Running Time: 21:23
Philip Lightfoot, B.S., B.A.
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Unit 3
Information Resources for Clinical Research
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Running Time: 58:09
Josh Duberman, M.L.I.S.
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Download Materials - Guidelines for Comprehensive Search Mount Sinai
Download Materials - Responsible Literature Searching Guidelines University of Pittsburgh
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Unit 4
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Unit 5
Design of Case Report Forms
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Running Time: 58:41
David Mailhot, B.S., M.P.H.
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Unit 6
NIH Peer Review Process
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Running Time: 1:06:42
Olivia Preble-Bartlett, Ph.D.
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Unit 7
Evaluation of Alternative and Complementary Therapies
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Running Time: 1:26:34
Marc Blackman, M.D.
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Unit 8
Inclusion of Women and Minorities in Clinical Trials
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Running Time: 38:15
Miriam Kelty, Ph.D.
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Product Development: Moving from the Bench to the Clinic
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Running Time: 42:09
Richard Schwartz, Ph.D.
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Unit 9
Technology Transfer
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Running Time: 58:17
Bruce Goldstein, J.D., M.S.
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Clinical Research From the Patient's Perspective
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Running Time: 63 minutes
Susan Lowell Butler, B.A., M.A.
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